Primary cardiac sarcomas constitute a rare entity that have been uniformly associated with poor long-term survival. A case of left atrial leiomyosarcoma involving the interatrial septum and the right atrial free wall and presenting with syncope and atrial fibrillation, is described. Two extensive surgical excisions followed by adjuvant radiation and chemotherapy improved survival with a good quality of life. This approach of combined surgical, medical and radiation therapy may offer better longterm outcome, since our patient is the longest survivor thus far reported
A 38-year-old woman had developed an abdominal distention, lower extremity edema, and dyspnea. Imagi...
Copyright © 2012 Philemon Gukop et al. This is an open access article distributed under the Creative...
Primary cardiac malignancies are rare entities. Although sarcomas enclosed the main group of maligna...
Primary leiomyosarcoma of the heart is uncommon and we were able to find only 15 cases reported in t...
Aim To present a rare case of cardiac sarcoma. Methods Clinical case of a 48-year-old female with dy...
Primary cardiac leiomyosarcoma is one of the rare primary malign cardiac tumors and it has a poor pr...
Leiomyosarcomas (LMS) of the heart are exceptional primary malignant tumours with a catastrophic pro...
Primary cardiac tumours are rare and frequently only diagnosed post-mortem. Recent improvements in n...
Abstract Primary cardiac sarcomas are rare tumors with an unfavourable prognosis. Complete surgical ...
Primary cardiac neoplasms are rare with an estimated prevalence of 0.001%–0.2%. Cardiac tumors are m...
Abstract Background Malignant primary cardiac tumors are infrequent and can lead to an unfavorable p...
Leiomyosarcoma of the heart is an uncommon primary malignant tumor with poor postoperative survival ...
Background Primary cardiac tumors are extremely rare. Most primary cardiac tumors are benign and aro...
We report a case of a 23-year-old man affected with dyspnea at rest, cough, and syncope. In the last...
Excision of a predominantly intracavitary right atrial tumor, which mimicked a number ofother clinic...
A 38-year-old woman had developed an abdominal distention, lower extremity edema, and dyspnea. Imagi...
Copyright © 2012 Philemon Gukop et al. This is an open access article distributed under the Creative...
Primary cardiac malignancies are rare entities. Although sarcomas enclosed the main group of maligna...
Primary leiomyosarcoma of the heart is uncommon and we were able to find only 15 cases reported in t...
Aim To present a rare case of cardiac sarcoma. Methods Clinical case of a 48-year-old female with dy...
Primary cardiac leiomyosarcoma is one of the rare primary malign cardiac tumors and it has a poor pr...
Leiomyosarcomas (LMS) of the heart are exceptional primary malignant tumours with a catastrophic pro...
Primary cardiac tumours are rare and frequently only diagnosed post-mortem. Recent improvements in n...
Abstract Primary cardiac sarcomas are rare tumors with an unfavourable prognosis. Complete surgical ...
Primary cardiac neoplasms are rare with an estimated prevalence of 0.001%–0.2%. Cardiac tumors are m...
Abstract Background Malignant primary cardiac tumors are infrequent and can lead to an unfavorable p...
Leiomyosarcoma of the heart is an uncommon primary malignant tumor with poor postoperative survival ...
Background Primary cardiac tumors are extremely rare. Most primary cardiac tumors are benign and aro...
We report a case of a 23-year-old man affected with dyspnea at rest, cough, and syncope. In the last...
Excision of a predominantly intracavitary right atrial tumor, which mimicked a number ofother clinic...
A 38-year-old woman had developed an abdominal distention, lower extremity edema, and dyspnea. Imagi...
Copyright © 2012 Philemon Gukop et al. This is an open access article distributed under the Creative...
Primary cardiac malignancies are rare entities. Although sarcomas enclosed the main group of maligna...